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dc.contributor.authorBronberg, Rubénes
dc.contributor.authorGroisman, Borises
dc.contributor.authorBidondo, María Pazes
dc.contributor.authorBarbero, Pabloes
dc.contributor.authorLiascovich, Rosaes
dc.date.accessioned2022-07-19T14:19:50Z-
dc.date.available2022-07-19T14:19:50Z-
dc.date.issued2020-07-
dc.identifier.issn1868-310X-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/2444-
dc.descriptionFil: Bronberg, Rubén. Ramos Mejía Hospital, Buenos Aires, Argentina /National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina /Buenos Aires Government Research Committee, Buenos Aires, Argentina.es
dc.descriptionFil: Groisman, Boris. National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina / National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.es
dc.descriptionFil: Bidondo, María Paz. National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina / Medicine College, University of Buenos Aires (UBA), Buenos Aires, Argentina.es
dc.descriptionFil: Barbero, Pablo. National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina.es
dc.descriptionFil: Liascovich, Rosa. National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina /National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.es
dc.description.abstractThe goal of our study is to describe the prevalence of congenital anomalies (CA) in hospitals of the City of Buenos Aires, Argentina, according to two proxy variables of the socioeconomic level: health subsector, public (PUB) versus private/social security (PRI), and geographical location, northern (N) versus southern (S). The source of data was the National Network of Congenital Anomalies of Argentina (RENAC) (period 2010-2016). From a total of 228,208 births, 4872 newborns with CA were detected (2.14%). The prevalence in PRI-N, PUB-N, PRI-S, and PUB-S hospitals were 1.59%, 1.91%, 2.20%, and 2.43%, respectively. Prevalence of neural tube defects, abdominal wall defects, and oral clefts was significantly higher in PUB than in PRI hospitals. Prevalence of critical heart defects was significantly lower in PUB-N and in PRI-S hospitals. Prevalence of anencephaly, encephalocele, hydrocephalus, microcephaly, gastroschisis, cleft lip and palate, ductus arteriosus, and bilateral renal agenesis was higher in PUB hospitals, both N and S, as well as microphthalmia/anophthalmia and ambiguous genitalia, spina bifida, anotia/microtia, postaxial polydactyly, and diaphragmatic hernia had higher prevalences in PUB-S hospitals. Omphalocele was more frequent in PUB-N hospitals. Results suggest that vulnerable populations in the public and southern subsectors of the city still require a greater support to reinforce resources and strategies that lead to greater equity in access to health.es
dc.language.isoenes
dc.publisherJ Community Genetes
dc.relation.ispartofJournal of community geneticses
dc.subjectArgentinaes
dc.subjectCongenital Abnormalitieses
dc.subjectSocial Classes
dc.subjectCitieses
dc.titleBirth prevalence of congenital anomalies in the City of Buenos Aires, Argentina, according to socioeconomic leveles
dc.typeArtículoes
dc.identifier.doi10.1007/s12687-019-00449-0-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.openairetypeArtículo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptCentro Nacional de Genética Médica (CeNaGeM)-
crisitem.author.deptRegistro Nacional de Anomalías Congénitas (RENAC)-
crisitem.author.deptCentro Nacional de Genética Médica (CeNaGeM)-
crisitem.author.deptRegistro Nacional de Anomalías Congénitas (RENAC)-
crisitem.author.deptCentro Nacional de Genética Médica (CeNaGeM)-
crisitem.author.deptRegistro Nacional de Anomalías Congénitas (RENAC)-
crisitem.author.deptCentro Nacional de Genética Médica (CeNaGeM)-
crisitem.author.deptRegistro Nacional de Anomalías Congénitas (RENAC)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Epidemiología (INE)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Epidemiología (INE)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Epidemiología (INE)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Epidemiología (INE)-
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